Tment diversity stems from our acquiring that C. elegans ARL-13 extends towards the ciliary strategies of young larval cilia, ahead of restricting to a proximal domain. Hence, the ARL13B/ ARL-13 PRIMA-1 web domain is differentially defined in distinctive cell types and at unique developmental stages, reflecting age and cell subtypespecific needs for this G-protein. Yet another interesting age distinction is the fact that we have only observed IFT-like motility for ARL-13 in young larval worms and not in later larvae or adults. Though there can be technical considerations that stop us seeing ARL-13 processive movement in older worms (e.g., larger levels of diffusing signals obscuring IFT movements), our data indicates that as the cilium ages, the proportion of ARL-13 undergoing active transport may perhaps lower in comparison with the fraction undergoing diffusion. Hence, for ciliary membrane proteins thought of as prospective IFT cargo, it may be fruitful to execute experiments on developing or newly formed cilia.MKS/NPHP modules and DYF-13 regulate the ARL-13 diffusion barrier at the TZOur function showing that ARL-13 readily diffuses in the middle segment membrane but fails to enter the adjacent TZ membrane subdomain clearly demonstrates an ARL-13 diffusion barrier in the C. elegans TZ. Utilizing subcellular localisation and in vivo FRAP assays we were then in a position to show that this barrier is bidirectional and dependent on MKS and NPHP genes, but not most IFT genes. These observations are constant with and extend published findings implicating a membrane diffusion barrier in the ciliary base, including a prior report by us and other folks showing that plasma membrane-associated RPI-2 (retinitis pigmentosa gene two orthologue) and transmembrane TRAM-1 (Sec61 ER translocon component) abnormally leak into the ciliary axonemes of TZ gene-disrupted worms [169,21]. Certainly, our improvement of the initially in vivo FRAP assay to measure barrier integrity and ciliary/periciliary exchange kinetics will help additional dissection of ciliary `gating’ in the TZ. Not all MKS, NPHP and IFT genes neatly match our model, nonetheless. By way of example, the ARL-13 barrier seems largely intact in TZ-associated nphp-4 single mutants, in spite of previous findings that non-ciliary plasma transmembrane and membrane-associated proteins (RPI-2, TRAM-1) abnormally leak in to the cilia of these worms [19]. Hence, NPHP-4 possesses selective `gating’ functions, necessary to prevent RPI-2 entry into cilia but not ARL-13 exit from cilia. In contrast, MKS-5 facilitates each these functions, indicating a extra global function in TZ barrier regulation. A further instance is dyf-13/TTC26, which is genetically and biochemically related together with the IFT-B complex [45,56,57]. As opposed to other IFT mutants we tested, the TZ barrier is moderately disrupted in dyf-13 single mutants, and also further compromised in dyf-13;nphp-4 double mutants, suggesting a synthetic functional partnership among these genes. In C. elegans, DYF-13 has been placed in a distinct OSM-3/KIF17 accessory motor module with DYF-1/IFT70, around the basis that it is essential for constructing a minimum of a part of the ciliary distal segment [45]. Surprisingly, although DYF13 undergoes IFT [58], it is actually not yet known if this protein is essential for IFT; thus it truly is achievable that DYF-13 is peripherally related with IFT complexes as a TZ-interacting cargo element, as opposed to a core element of the IFT machinery.